Evidence map›Paper›PMID 38443525›Full record

ArticlePediatric research2024

Increased mortality in infants with abnormal T-cell receptor excision circles.

Jenny Huang, Ashwin Shankar, Isabel Hurden, Ronald Thomas, Joseph Hill, Divya Seth, Elizabeth Secord, Pavadee Poowuttikul

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 47% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Transient B cell lymphopenia revealed by KRECs newborn screening: Post-screening referral strategies, clinical course, and follow-up.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Article
  2. First pilot study for newborn screening of severe T and B lymphopenias in ColombiaBiomedica : revista del Instituto Nacional de Salud · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Jenny HuangDepartment of Pediatrics, Division of Allergy/Immunology, Children's Hospital of Michigan, Detroit, MI, USA.
Ashwin ShankarDepartment of Pediatrics, Division of Allergy/Immunology, Children's Hospital of Michigan, Detroit, MI, USA.
Isabel HurdenMichigan Department of Health and Human Services, Lansing, MI, USA.
Ronald ThomasCentral Michigan University, College of Medicine, Mt. Pleasant, MI, USA.
Joseph HillMichigan Department of Health and Human Services, Lansing, MI, USA.
Divya SethDepartment of Pediatrics, Division of Allergy/Immunology, Children's Hospital of Michigan, Detroit, MI, USA.
Elizabeth SecordWayne State University, School of Medicine, Detroit, MI, USA.
Pavadee PoowuttikulDepartment of Pediatrics, Division of Allergy/Immunology, Children's Hospital of Michigan, Detroit, MI, USA. ppoowutt@dmc.org.
Central Michigan University · USChildren's Hospital of Michigan · USMichigan Department of Health and Human Services · USWayne State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundT-Cell Receptor Excision Circles based newborn screening (TREC-NBS) allows for early detection of T-cell lymphopenia in infants with primary immunodeficiency disorders (PIDD). The utility of abnormal TREC-NBS in infants without PIDD is not well studied. We sought to evaluate the association of abnormal TREC-NBS with mortality.

methods365,207 TREC-NBS from October 2011 to December 2014 were reviewed. 467 newborns had abnormal screens and did not meet the criteria for a PIDD diagnosis. Cases were matched to controls (1:3) based on gestational age, birth weight, neonatal intensive care unit status (NICU), and race. Data were obtained through NBS, birth and death certificates records from the Michigan Department of Health and Human Services (MDHHS) databases.

resultsInfants with abnormal TREC-NBS had higher mortality even when PIDD was ruled-out. Transient abnormal TREC-NBS was not associated with higher mortality, but unresolved or late abnormal TREC-NBS was associated with higher mortality. Infants with late abnormal TREC-NBS had severe prematurity, lower birth weight, lower Apgar scores, and higher percentage of congenital anomalies.

conclusionInfants with abnormal TREC-NBS may be at a higher risk of morbidity and mortality and should be carefully followed, especially if discharged home before a repeat screen can be completed. IMPACT: This study explores the risk factors and mortality for newborns with secondary T-cell lymphopenia captured on T-Cell Receptor Excision Circles based newborn screening (TREC-NBS). Abnormal TREC-NBS allows for prompt life-saving interventions for primary immunological conditions such as Severe Combined Immunodeficiency (SCID), but can also be associated with non-immunologic conditions. Unresolved and late abnormal TREC-NBS is associated with higher mortality even without primary immunodeficiency, likely detected in infants with more severe prematurity, lower birth weight, and congenital anomalies. TREC-NBS positive infants with secondary T-cell lymphopenia require special attention and close monitoring.

Indexed as

LymphopeniaNeonatal ScreeningReceptors, Antigen, T-CellBirth WeightCase-Control StudiesFemaleGestational AgeHumansInfantInfant, NewbornMaleMichiganRetrospective StudiesRisk FactorsT-LymphocytesReceptors, Antigen, T-Cell

Identifiers

PMID38443525
OpenAlexW4392450489

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.